Evaluation of parallel operated small-scale bubble columns for microbial process development using Staphylococcus carnosus

被引:12
作者
Dilsen, S
Paul, W
Herforth, D
Sandgathe, A
Altenbach-Rehm, J
Freudl, R
Wandrey, C
Weuster-Botz, D
机构
[1] Forschungszentrum Julich, Inst Biotechnol, D-52425 Julich, Germany
[2] Univ Dusseldorf, Inst Enzymtechnol, D-52425 Julich, Germany
关键词
small-scale bubble columns; shake flasks; parallel pH-control; Staphylococcus carnosus; human calcitonin;
D O I
10.1016/S0168-1656(01)00265-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Shake flasks and pH-controlled small-scale bubble columns were compared with respect to their usefulness as a basic tool for process development for human calcitonin precursor fusion-protein production with Staphylococcus carnosus. Parallel control of the pH land making use of the base addition data) is necessary to study the effects of medium composition, to identify pH-optima and to develop a medium, which minimizes the acid excretion of S. carnosus. This medium with glycerol as energy source and yeast extract as carbon and nitrogen source resulted in cell dry weight concentration in shake flasks of 5 g l(-1), which were thus improved by a factor of 10. Cell dry weight concentrations of up to 12.5 g l(-1) were measured in the batch process with pH-controlled small-scale bubble columns due to their higher oxygen transfer capability. In contrast to shake flasks it was demonstrated, that the batch process performance of recombinant S. carnosus secreting the human calcitonin precursor fusion-protein was identical within the estimation error in pH-controlled small-scale bubble columns compared to the stirred-tank reactor. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
相关论文
共 17 条
[1]  
Altenbach-Rehm J, 1999, CHEM ENG TECHNOL, V22, P1051, DOI 10.1002/(SICI)1521-4125(199912)22:12<1051::AID-CEAT1051>3.0.CO
[2]  
2-C
[3]   Fed-batch production of recombinant human calcitonin precursor fusion protein using Staphylococcus carnosus as an expression-secretion system [J].
Dilsen, S ;
Paul, W ;
Sandgathe, A ;
Tippe, D ;
Freudl, R ;
Thömmes, J ;
Kula, MR ;
Takors, R ;
Wandrey, C ;
Weuster-Botz, D .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2000, 54 (03) :361-369
[4]  
DRESCHER T, 1999, Patent No. 19709603
[5]  
FALK MPF, 1991, APPL MICROBIOL BIOT, V35, P10
[6]   APPLIED GENETICS IN THE GRAM-POSITIVE BACTERIUM STAPHYLOCOCCUS-CARNOSUS [J].
GOTZ, F .
FOOD BIOTECHNOLOGY, 1990, 4 (01) :505-513
[7]   SUITABILITY OF THE SHAKING FLASK FOR OXYGEN-SUPPLY TO MICROBIOLOGICAL CULTURES [J].
HENZLER, HJ ;
SCHEDEL, M .
BIOPROCESS ENGINEERING, 1991, 7 (03) :123-131
[8]   LIPASE PRODUCTION OF STAPHYLOCOCCUS-CARNOSUS IN A DIALYSIS FERMENTER [J].
LECHNER, M ;
MARKL, H ;
GOTZ, F .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1988, 28 (4-5) :345-349
[9]   Use of the pre-pro part of Staphylococcus hyicus lipase as a carrier for secretion of Escherichia coli outer membrane protein A (OmpA) prevents proteolytic degradation of OmpA by cell-associated protease(s) in two different gram-positive bacteria [J].
Meens, J ;
Herbort, M ;
Klein, M ;
Freudl, R .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (07) :2814-2820
[10]   PRODUCTION OF THE IMMUNOGLOBULIN VARIABLE DOMAIN REI(V) VIA A FUSION PROTEIN SYNTHESIZED AND SECRETED BY STAPHYLOCOCCUS-CARNOSUS [J].
PSCHORR, J ;
BIESELER, B ;
FRITZ, HJ .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1994, 375 (04) :271-280